(4Z)-2-methyl-4-(5-phenyl-1,2-oxazolidin-3-ylidene)cyclohexa-2,5-dien-1-one

Details

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Internal ID 793d50bd-0f15-4524-9b91-e35d665a1c41
Taxonomy Organoheterocyclic compounds > Azolidines > Isoxazolidines > Phenylisoxazolidines
IUPAC Name (4Z)-2-methyl-4-(5-phenyl-1,2-oxazolidin-3-ylidene)cyclohexa-2,5-dien-1-one
SMILES (Canonical) CC1=CC(=C2CC(ON2)C3=CC=CC=C3)C=CC1=O
SMILES (Isomeric) CC1=C/C(=C\2/CC(ON2)C3=CC=CC=C3)/C=CC1=O
InChI InChI=1S/C16H15NO2/c1-11-9-13(7-8-15(11)18)14-10-16(19-17-14)12-5-3-2-4-6-12/h2-9,16-17H,10H2,1H3/b14-13-
InChI Key PESGIJSKABCHLK-YPKPFQOOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H15NO2
Molecular Weight 253.29 g/mol
Exact Mass 253.110278721 g/mol
Topological Polar Surface Area (TPSA) 38.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4Z)-2-methyl-4-(5-phenyl-1,2-oxazolidin-3-ylidene)cyclohexa-2,5-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8562 85.62%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6667 66.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9421 94.21%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5591 55.91%
P-glycoprotein inhibitior - 0.8591 85.91%
P-glycoprotein substrate - 0.7966 79.66%
CYP3A4 substrate + 0.5138 51.38%
CYP2C9 substrate - 0.5844 58.44%
CYP2D6 substrate - 0.8448 84.48%
CYP3A4 inhibition - 0.7370 73.70%
CYP2C9 inhibition + 0.5670 56.70%
CYP2C19 inhibition + 0.7066 70.66%
CYP2D6 inhibition - 0.8499 84.99%
CYP1A2 inhibition + 0.6062 60.62%
CYP2C8 inhibition - 0.8281 82.81%
CYP inhibitory promiscuity + 0.9235 92.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Danger 0.3739 37.39%
Eye corrosion - 0.9816 98.16%
Eye irritation - 0.9044 90.44%
Skin irritation - 0.7542 75.42%
Skin corrosion - 0.9292 92.92%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8538 85.38%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7633 76.33%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5488 54.88%
Acute Oral Toxicity (c) III 0.6743 67.43%
Estrogen receptor binding + 0.7303 73.03%
Androgen receptor binding + 0.5485 54.85%
Thyroid receptor binding - 0.6275 62.75%
Glucocorticoid receptor binding - 0.7327 73.27%
Aromatase binding + 0.6714 67.14%
PPAR gamma - 0.7252 72.52%
Honey bee toxicity - 0.9551 95.51%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.4013 40.13%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.87% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.61% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.31% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.62% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.06% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.99% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.12% 91.11%
CHEMBL4208 P20618 Proteasome component C5 81.09% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.15% 85.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Angelica sinensis
Artemisia capillaris
Bupleurum chinense
Clematis chinensis
Juncus effusus
Panax quinquefolius
Vitex trifolia

Cross-Links

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PubChem 49771170
NPASS NPC103497